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FDA 510(k)

SUPPLEMENTAL FEEDING SYSTEM

K-Number: K844297 · 1985-02-25

ApplicantMedela, Inc.
Decision Date1985-02-25
Product CodeHGY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SUPPLEMENTAL FEEDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medela, Inc.. It received FDA 510(k) clearance on 1985-02-25 under 510(k) number K844297. The device is classified under product code HGY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPPLEMENTAL FEEDING SYSTEM?

SUPPLEMENTAL FEEDING SYSTEM is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Medela, Inc.. The 510(k) number is K844297.

When did SUPPLEMENTAL FEEDING SYSTEM receive FDA 510(k) clearance?

SUPPLEMENTAL FEEDING SYSTEM received FDA 510(k) clearance on 1985-02-25, under 510(k) number K844297.

Who is the listed applicant for SUPPLEMENTAL FEEDING SYSTEM?

The FDA 510(k) record lists Medela, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPPLEMENTAL FEEDING SYSTEM?

The FDA product code for SUPPLEMENTAL FEEDING SYSTEM is HGY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medela, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 19 devices →

Related Devices (Code: HGY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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